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Consent for Use of Personal Information
for Program Evaluation
In order to assess the effectiveness of the Guided Application (GAP) session, the
Outreach staff of Nova Scotia Student Assistance, Nova
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How to fill out informed consent guidance
How to fill out informed consent guidance
01
Start by reviewing the informed consent form provided by your organization or institution.
02
Read through the entire form carefully and make sure you understand each section and requirement.
03
Consult with your supervisor or ethics committee if you have any questions or need clarification.
04
Ensure that all necessary information is included in the form, such as the purpose of the research, potential risks and benefits, confidentiality measures, and participant rights.
05
Provide a detailed explanation of the research procedures and ensure that participants understand what they will be involved in.
06
Clearly outline any compensation or incentives that participants may receive for their participation.
07
Obtain written consent from the participants and ensure that they have had enough time to review the form and ask any questions.
08
Keep a copy of the informed consent form for your records and provide a copy to the participant as well.
09
Regularly revisit and update the informed consent process as needed, especially if there are any changes to the research study or participant rights.
10
Be available to address any concerns or questions from participants throughout the research study.
Who needs informed consent guidance?
01
Researchers conducting human subjects research
02
Healthcare professionals conducting medical procedures or treatments
03
Psychologists or therapists working with clients
04
Educational institutions conducting research on students
05
Non-profit organizations conducting research on beneficiaries
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What is informed consent guidance?
Informed consent guidance refers to the protocols and regulations ensuring that individuals understand the risks, benefits, and purpose of a procedure or participation in research before giving their consent.
Who is required to file informed consent guidance?
Researchers, healthcare providers, and institutions conducting studies or medical procedures that involve human subjects are required to file informed consent guidance.
How to fill out informed consent guidance?
Informed consent guidance is typically filled out by completing a form that outlines the study or procedure details, risks and benefits, confidentiality, and giving participants space to ask questions before signing.
What is the purpose of informed consent guidance?
The purpose of informed consent guidance is to ensure that individuals have ample information to make an educated decision about their participation in research or medical procedures.
What information must be reported on informed consent guidance?
Information that must be reported includes the purpose of the study, procedures involved, risks and benefits, confidentiality measures, and the right to withdraw consent at any time.
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